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在接受晚期生殖细胞肿瘤治疗的患者中,高累积剂量依托泊苷后发生的继发性白血病。

Secondary leukemia following high cumulative doses of etoposide in patients treated for advanced germ cell tumors.

作者信息

Kollmannsberger C, Beyer J, Droz J P, Harstrick A, Hartmann J T, Biron P, Fléchon A, Schöffski P, Kuczyk M, Schmoll H J, Kanz L, Bokemeyer C

机构信息

Department of Hematology/Oncology, University of Tuebingen Medical Center, Germany.

出版信息

J Clin Oncol. 1998 Oct;16(10):3386-91. doi: 10.1200/JCO.1998.16.10.3386.

Abstract

PURPOSE

High cumulative epipodophyllotoxin dosages are reported to be associated with an elevated risk for secondary acute myeloid leukemia (s-AML). This study examined the risk of s-AML following cumulative etoposide doses greater than 2 g/m2 in patients with metastatic germ cell tumors (GCT).

PATIENTS AND METHODS

The incidence of s-AML was retrospectively assessed in patients treated within clinical trials between January 1986 and February 1996 at four university centers. All patients received high-dose chemotherapy (HDCT) plus autologous stem-cell support for metastatic GCT, including high cumulative etoposide doses (> 2 g/m2). Minimum patient follow-up was 12 months. Standardized morbidity ratio (SMR) was calculated to estimate the risk associated with high cumulative etoposide doses, as compared with the general population.

RESULTS

A total of 302 patients with a median age of 29 years (range, 15 to 55) received a median cumulative etoposide dose of 5 g/m2 (range, 2.4 to 14 g/m2). Four cases of s-AML were observed, which resulted in a cumulative incidence of 1.3% (95% confidence interval [CI], 0.38% to 3.59%) at 52 months of median follow-up (range, 12 to 198). Two cases of secondary myelodysplasia (s-MDS) developed in patients with primary mediastinal GCT. Based on the observed four cases of AML, which are most likely etoposide-related, the risk for developing s-AML (SMR, 160 [95% CI, 43.7 to 411.2]) is significantly increased in comparison to the age-matched general population.

CONCLUSION

Due to the low incidence of AML in the general population, the significantly elevated risk for developing s-AML affects only 1.3% of all patients who receive etoposide doses greater than 2 g/m2. HDCT, including etoposide doses greater than 2 g/m2, is associated with an acceptably low incidence of s-AML in patients with advanced GCT.

摘要

目的

据报道,高累积剂量的表鬼臼毒素与继发性急性髓系白血病(s-AML)风险升高有关。本研究调查了转移性生殖细胞肿瘤(GCT)患者在累积依托泊苷剂量大于2 g/m²后发生s-AML的风险。

患者与方法

回顾性评估1986年1月至1996年2月期间在四个大学中心进行的临床试验中接受治疗的患者发生s-AML的情况。所有患者均接受了高剂量化疗(HDCT)加自体干细胞支持治疗转移性GCT,包括高累积依托泊苷剂量(>2 g/m²)。患者最短随访时间为12个月。计算标准化发病比(SMR)以估计与高累积依托泊苷剂量相关的风险,并与普通人群进行比较。

结果

共有302例患者,中位年龄29岁(范围15至55岁),中位累积依托泊苷剂量为5 g/m²(范围2.4至14 g/m²)。观察到4例s-AML,中位随访52个月(范围12至198个月)时累积发病率为1.3%(95%置信区间[CI],0.38%至3.59%)。2例原发性纵隔GCT患者发生了继发性骨髓发育异常(s-MDS)。基于观察到的4例最可能与依托泊苷相关的AML病例,与年龄匹配的普通人群相比,发生s-AML的风险(SMR,160[95%CI,43.7至411.2])显著增加。

结论

由于普通人群中AML发病率较低,s-AML发生风险显著升高仅影响所有接受依托泊苷剂量大于2 g/m²患者中的1.3%。包括依托泊苷剂量大于2 g/m²的HDCT与晚期GCT患者中s-AML的低发病率相关,该发病率可接受。

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